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Molecular screening for fragile X syndrome in children with unexplained intellectual disability and/or autistic behaviour.

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INTRODUCTION Fragile X syndrome (FXS, OMIM #300624) is the most common inherited form of intellectual disability and the leading monogenic cause of autism. Click to show full abstract

INTRODUCTION Fragile X syndrome (FXS, OMIM #300624) is the most common inherited form of intellectual disability and the leading monogenic cause of autism.

Keywords: intellectual disability; screening fragile; molecular screening; syndrome children; fragile syndrome

Journal Title: Folia medica
Year Published: 2022

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